Copper acetate monohydrate - ≥99.95% metals basis , CAS No.6046-93-1

CAS: 6046-93-1 Cat. No.: C108085 Summenformel: C4H6CuO4·H2O Molekulargewicht: 199.65 Beilstein Registry Number: 3730548 EG-Nummer: 611-978-9
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QUALITÄT & REINHEIT ≥99.95% metals basis
Synonyms
Copper(II) Acetate Monohydrate | Acetic Acid Copper(II) Salt Monohydrate
Storage
Room temperature
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Warum diese Qualität

≥99.95% metals basis für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Literaturbeleg

In 428 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Spezifikationen

Synonyme
Copper(II) Acetate Monohydrate | Acetic Acid Copper(II) Salt Monohydrate
Spezifikationen & Reinheit
≥99.95% metals basis
Storage
Room temperature
Verschickt in
Normal
Reinheit
≥99.95% metals basis
Namen und Kennungen
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508811966
Kanonisches Lächeln
CC(=O)[O-].CC(=O)[O-].O.[Cu+2]
IUPAC Name
copper;diacetate;hydrate
InChIKey
NWFNSTOSIVLCJA-UHFFFAOYSA-L
INCHI
1S/2C2H4O2.Cu.H2O/c2*1-2(3)4;;/h2*1H3,(H,3,4);;1H2/q;;+2;/p-2
Isomere SMILES
CC(=O)[O-].CC(=O)[O-].O.[Cu+2]
WGK Deutschland
3
RTECS
AG3500000
UN-Nummer
3077
Verpackungsgruppe
II
Molekulargewicht
199.65
Beilstein
3730548
Reaxy-Rn
3730548
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3730548&ln=

Dokumentation

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✅ Analysezertifikat (COA)

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
KlasseCarboxylic acids and derivatives
SubclassCarboxylic acid derivatives
Intermediate Tree Nodes Carboxylic acid salts
Direct ParentAcetate salts
Alternative Parents Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Organic copper salts  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkNot available
Substituents Acetate salt - Organic transition metal salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic copper salt - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as acetate salts. These are organic compounds containing acetic acid as its acid component.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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33 results found

Lot NumberCertificate TypeDatumArtikel
A2305495A2305495Certificate of AnalysisSep 22, 2026 C108085
A2305496A2305496Certificate of AnalysisSep 22, 2026 C108085
A2305498A2305498Certificate of AnalysisSep 22, 2026 C108085
L2210432L2210432Certificate of AnalysisSep 01, 2026 C108085
J2612256J2612256Certificate of AnalysisJan 09, 2026 C108085
G2602332G2602332Certificate of AnalysisJan 09, 2026 C108085
B2625454B2625454Certificate of AnalysisJan 09, 2026 C108085
B2625428B2625428Certificate of AnalysisJan 09, 2026 C108085
B2625427B2625427Certificate of AnalysisJan 09, 2026 C108085
J2612285J2612285Certificate of AnalysisJan 09, 2026 C108085
J2612279J2612279Certificate of AnalysisJan 09, 2026 C108085
K2519274K2519274Certificate of AnalysisNov 10, 2025 C108085
K2519300K2519300Certificate of AnalysisNov 10, 2025 C108085
K2519292K2519292Certificate of AnalysisNov 10, 2025 C108085
F2526229F2526229Certificate of AnalysisJun 12, 2025 C108085
F2526232F2526232Certificate of AnalysisJun 12, 2025 C108085
F2526233F2526233Certificate of AnalysisJun 12, 2025 C108085
L2210431L2210431Certificate of AnalysisNov 08, 2022 C108085
A2305489A2305489Certificate of AnalysisNov 08, 2022 C108085
L2210433L2210433Certificate of AnalysisNov 08, 2022 C108085
L2210434L2210434Certificate of AnalysisNov 08, 2022 C108085
L2210435L2210435Certificate of AnalysisNov 08, 2022 C108085
F2502136F2502136Certificate of AnalysisNov 08, 2022 C108085
A2305487A2305487Certificate of AnalysisNov 08, 2022 C108085
I2214386I2214386Certificate of AnalysisJun 09, 2022 C108085
I2214380I2214380Certificate of AnalysisJun 09, 2022 C108085
I2214379I2214379Certificate of AnalysisJun 09, 2022 C108085
I2214372I2214372Certificate of AnalysisJun 09, 2022 C108085
I2214371I2214371Certificate of AnalysisJun 09, 2022 C108085
I2214370I2214370Certificate of AnalysisJun 09, 2022 C108085
B2209020B2209020Certificate of AnalysisDec 14, 2021 C108085
B2209019B2209019Certificate of AnalysisDec 14, 2021 C108085
B2209017B2209017Certificate of AnalysisDec 14, 2021 C108085
Chemische und physikalische Eigenschaften
EmpfindlichkeitMoisture sensitive.
Schmelzpunkt (°C)240 °C
Molekulargewicht199.650 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count5
Rotatable Bond Count0
Exact Mass198.967 Da
Monoisotopic Mass198.967 Da
Topological Polar Surface Area81.300 Ų
Heavy Atom Count10
Formal Charge0
Complexity25.500
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count4
FAQs und Artikel
Chemical Synthesis Methods of Nanomaterials
Dimethoxymethylsilane, DMMS
PMHS, Polymethylhydrosiloxane
TEMPO-Catalyzed Oxidation Quick Reference (Alcohol Oxidation Focus): Three Regeneration Routes (NaOCl / Cu–O₂ / PIDA) + Selection & Troubleshooting
Transition-Metal Salts/Precursor Selection Guide: How “Different Salts of the Same Metal” Start from Different Chemical Realities—and How to Reproduce Results (including a Selection Navigator and Product Tables 1–5)
Experimental Selection Logic for C-C Bond Construction: Understanding Fragment Coupling, Carbonyl Chain Extension, Olefination, and Late-Stage Bond-Forming Pathways by Bond-Forming Task
Reaction Selection in Small-Molecule Synthesis: From Transformation-Type Assessment to Experimental Route Screening
Experimental Selection Logic for Transition-Metal-Catalyzed C–H Functionalization: When It Is Worth Pursuing and How to Assess Site Selectivity and Conditions
Copper Tripeptide GHK-Cu and Skin Repair: From Copper Coordination Chemistry to Extracellular Matrix Remodeling
Why Do Skincare Oligopeptides Have Different Effects? — Molecular Structure, Skin Delivery, and Mechanisms of Action
Citations of This Product
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